A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism

Soysal, Yasemin ; Vermeesch, Joris ; Davani, Nooshin Ardeshir ; Hekimler, Kuyaş ; İmirzalıoğlu, Necat

American Journal of Medical Genetics Part A, 2011, Vol.155A (7), p.1745-1752

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